A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024176



Internal ID19113393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:20886606..21325152hg38UCSC Ensembl
Innerchr5:20886715..21325261hg19UCSC Ensembl
Innerchr5:20922472..21361018hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38438547
hg19438547
hg18438547
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5599n100
Supporting Variantsnssv3745835
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024176
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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